CN111849905A - Immunotherapy of mesenchymal stem cells targeting the transport of chemokines and cytokines - Google Patents

Abstract

The present invention provides immunotherapy of mesenchymal stem cells targeting chemokines and cytokines. Specifically, the present invention provides a mesenchymal stem cell, the mesenchymal stem cell expresses an immunostimulatory factor selected from the group consisting of CCL3, CCL19, CCL21, XCL1, CXCL9, OX40L, 4-1BBL , GITRL, CD40L, or a combination thereof. The mesenchymal stem cells of the present invention can specifically attract and activate immune cells that kill tumor tissues at the tumor site, and the mesenchymal stem cells have a synergistic effect with chemokines and/or cytokines, and have more efficient and less side effects. , significantly enhanced the killing ability of tumor tissue, especially colorectal cancer cells.

Description

Immunotherapy of mesenchymal stem cells targeting the transport of chemokines and cytokines

technical field

The present invention pertains, in particular, to immunotherapy targeting mesenchymal stem cells for the delivery of chemokines and cytokines.

Background technique

The rapid development of immunotherapy has brought a new dawn to cancer, especially chimeric antigen receptor T-cell immunotherapy (CAR-T) and immune regulatory checkpoint blockade are two of the most advanced cancer immunotherapy. CAR-T cell therapy has shown certain efficacy in some types of cancer, but it has also encountered inefficiency of T cells reaching the solid tumor site and short duration of action, the number of existing immune cells in the tumor site is small, and systemic medication brings side effects etc. bottlenecks. The use of antibodies targeting the T cell inhibitory receptors PD-1 or CTLA-4 can produce very significant anti-tumor effects. However, the therapeutic efficacy of antibodies is often limited by a number of factors, such as low T cell infiltration and loss of activity in solid tumors. In addition, systemic use of immunotherapy drugs such as interferon alpha, interleukin 2 or PD-1 antibodies may cause serious side effects.

Therefore, there is an urgent need in the art for an immunotherapy that can specifically target tumor cells.

SUMMARY OF THE INVENTION

The purpose of the present invention is to provide an immunotherapy that can specifically target tumor cells.

Another object of the present invention is to provide an immunotherapy for mesenchymal stem cells to target and transport chemokines and cytokines.

A first aspect of the present invention provides a mesenchymal stem cell, the mesenchymal stem cell expresses an immune stimulatory factor selected from the group consisting of CCL3, CCL19, CCL21, XCL1, CXCL9, OX40L, 4 - 1BBL, GITRL, CD40L, or a combination thereof.

In another preferred embodiment, the mesenchymal stem cells contain an exogenous nucleic acid molecule, and the exogenous nucleic acid molecule includes a nucleic acid sequence encoding an immunostimulatory factor selected from the group consisting of CXCL9, OX40L, CCL3, CCL19, CCL21, XCL1, CXCL9, OX40L, 4-1BBL, GITRL, CD40L, or a combination thereof.

In another preferred embodiment, the exogenous nucleic acid molecule further comprises a promoter or a promoter/enhancer combination, and the nucleic acid sequence encoding an immunostimulatory factor is operably linked to the promoter or the promoter/enhancer combination.

In another preferred embodiment, the promoter is a constitutive promoter or an inducible promoter, preferably a constitutive promoter.

In another preferred embodiment, the immunostimulatory factor includes at least one chemokine, and the chemokine includes: CCL3, CCL19, CCL21, XCL1, CXCL9, or a combination thereof.

In another preferred embodiment, the immunostimulatory factor includes at least one cytokine, and the cytokine includes: OX40L, 4-1BBL, GITRL, CD40L, or a combination thereof.

In another preferred embodiment, the immunostimulatory factor includes at least one chemokine and at least one cytokine, wherein the chemokine includes: CCL3, CCL19, CCL21, XCL1, CXCL9, or a combination thereof, wherein The cytokines include: OX40L, 4-1BBL, GITRL, CD40L, or a combination thereof.

In another preferred embodiment, the immunostimulatory factor is one or both of CCL3, CCL19, CCL21, and XCL1 in combination with CD40L.

In another preferred embodiment, the immunostimulatory factor is one or both of OX40L, 4-1BBL, GITRL and CXCL9 in combination.

In another preferred example, the immunostimulatory factor is CXCL9 and/or OX40L.

In another preferred embodiment, the exogenous nucleic acid molecule includes a first expression cassette and/or a second expression cassette, the first expression cassette contains a nucleic acid sequence encoding a chemokine, and the second expression cassette contains a cell encoding The nucleic acid sequence of a factor, wherein the chemokine comprises: CCL3, CCL19, CCL21, XCL1, CXCL9, or a combination thereof, and the cytokine comprises: OX40L, 4-1BBL, GITRL, CD40L, or a combination thereof.

In another preferred embodiment, the exogenous nucleic acid molecule includes a first expression cassette and a second expression cassette, the first expression cassette contains a nucleic acid sequence encoding CXCL9, and the second expression cassette contains a nucleic acid sequence encoding OX40L.

In another preferred embodiment, the first expression cassette and the second expression cassette are independent of each other, or combined into one.

In another preferred embodiment, the first expression cassette and the second expression cassette further comprise a promoter and/or a terminator, respectively.

In another preferred embodiment, the first expression cassette and the second expression cassette are the same expression cassette, and the expression cassette comprises a promoter, a nucleic acid sequence encoding a chemokine and a nucleic acid sequence encoding a cytokine.

In another preferred embodiment, the first expression cassette and the second expression cassette are located on a vector or integrated into the chromosome of the mesenchymal stem cell.

In another preferred embodiment, the first expression cassette and the second expression cassette are independent or linked.

In another preferred embodiment, the first expression cassette and the second expression cassette are located on the same or different vectors.

In another preferred embodiment, the first expression cassette and the second expression cassette are located in the same vector.

In another preferred embodiment, the vector is selected from the group consisting of DNA, RNA, plasmid, lentiviral vector, adenoviral vector, retroviral vector, transposon, other gene transfer systems, or a combination thereof.

In another preferred example, the mesenchymal stem cells include: adipose-derived mesenchymal stem cells, umbilical cord mesenchymal stem cells, or a combination thereof.

In another preferred embodiment, the mesenchymal stem cells are ex vivo.

In another preferred embodiment, the mesenchymal stem cells are autologous or allogeneic.

The second aspect of the present invention provides a method for preparing the mesenchymal stem cells described in the first aspect of the present invention, comprising the following steps:

(1) providing a mesenchymal stem cell to be modified; and

(2) introducing an exogenous nucleic acid containing a nucleic acid sequence encoding an immunostimulatory factor into the mesenchymal stem cell to be transformed, thereby obtaining the mesenchymal stem cell according to the first aspect of the present invention;

Wherein, the immunostimulatory factor is selected from the group consisting of CCL3, CCL19, CCL21, XCL1, CXCL9, OX40L, 4-1BBL, GITRL, CD40L, or a combination thereof.

The third aspect of the present invention provides a preparation comprising the mesenchymal stem cells according to the first aspect of the present invention, and a pharmaceutically acceptable carrier, diluent or excipient.

In another preferred embodiment, the preparation is a liquid preparation.

In another preferred embodiment, the dosage form of the preparation includes injection.

In another preferred embodiment, the concentration of mesenchymal stem cells in the preparation is 1×10 ³ -1×10 ⁸ cells/ml, preferably 1×10 ⁴ -1×10 ⁷ cells/ml.

The fourth aspect of the present invention provides the use of the mesenchymal stem cells according to the first aspect of the present invention for preparing a medicament or preparation for preventing and/or treating cancer or tumor.

In another preferred embodiment, the tumor is selected from the group consisting of hematological tumors, solid tumors, or a combination thereof. Preferably, the tumor is a solid tumor.

In another preferred embodiment, the hematological tumor is selected from the group consisting of acute myeloid leukemia (AML), multiple myeloma (MM), chronic lymphocytic leukemia (CLL), acute lymphoblastic leukemia (ALL), diffuse B-cell lymphoma (DLBCL), or a combination thereof.

In another preferred embodiment, the solid tumor is selected from the group consisting of gastric cancer, gastric cancer peritoneal metastasis, liver cancer, leukemia, kidney tumor, lung cancer, small intestine cancer, bone cancer, prostate cancer, colorectal cancer, breast cancer, colorectal cancer, Cervical cancer, ovarian cancer, lymphoma, nasopharyngeal cancer, adrenal tumor, bladder tumor, non-small cell lung cancer (NSCLC), glioma, endometrial cancer, squamous cell carcinoma of the lung, anal cancer, head and neck cancer, or its combination.

In another preferred embodiment, the solid tumor is colorectal cancer.

The fifth aspect of the present invention provides a pharmaceutical combination, the pharmaceutical combination contains

(1) the mesenchymal stem cell according to the first aspect of the present invention; and

(2) Anti-tumor immunotherapy agents.

In another preferred embodiment, the anti-tumor immunotherapy agent is selected from the group consisting of antibodies, immune cells, or a combination thereof.

In another preferred embodiment, the immune cells are T cells or NK cells.

In another preferred embodiment, the anti-tumor immunotherapy agent is an immune checkpoint antibody.

In another preferred embodiment, the immune checkpoint antibody includes PD-1 antibody and/or CTLA-4 antibody.

The present invention also provides a method for treating a disease, comprising administering an appropriate amount of the cells of the first aspect of the present invention, or the preparation of the third aspect of the present invention, or the fifth aspect of the present invention to a subject in need of treatment. drug combination.

In another preferred embodiment, the disease is cancer or tumor, preferably solid tumor, more preferably colorectal cancer.

It should be understood that within the scope of the present invention, the above-mentioned technical features of the present invention and the technical features specifically described in the following (eg, the embodiments) can be combined with each other to form new or preferred technical solutions. Due to space limitations, it is not repeated here.

Description of drawings

Figure 1 shows the identification of mouse adipose-derived mesenchymal stem cell phenotype and tumor-migrating properties. A, The expression of surface molecules of adipose-derived mesenchymal stem cells was detected by flow cytometry. B, Migration of MSC-GFP in vivo in a CT26 subcutaneous xenograft mouse model. The infiltration of MSC-GFP in tumor tissue was detected by immunofluorescence, green indicates MSC-GFP, blue (DAPI staining) indicates nuclei, scale bar: 20 μM. C, The specific quantity of MSC-GFP in the whole CT26 subcutaneous xenograft was detected by flow cytometry. Data represent mean ± SEM (n=3).

Figure 2 shows that overexpression of CXCL9 in tumor cells inhibits tumor growth in vivo. A, WB and qPCR detection of CCL3 and CXCL9 overexpression in CT26. Data represent mean ± SEM (n=3). B, Cell proliferation assay of CT26-Vector, CT26-CCL3 and CT26-CXCL9. Data represent mean ± SEM (n=3). C, Tumor growth curve in BALB/c mice injected subcutaneously with CT26-Vector, CT26-CCL3 or CT26-CXCL9 tumor cells, and tumor size was measured every 3 days. Data represent mean ± SEM (n=4). D, Percentage of total intracellular CD8+, CD4+ T and NK cells. Data represent mean ± SEM (n=4).

Figure 3 shows that overexpression of OX40L in tumor cells inhibits tumor growth in vivo. A, WB detected the overexpression of IL36β and OX40L in CT26. B, Flow cytometry detection of OX40L overexpression in CT26. C, Cell proliferation assay of CT26-Vector, CT26-IL36β and CT26-OX40L. Data represent mean ± SEM (n=3). D, Tumor growth curves in BALB/c mice injected subcutaneously with CT26-Vector, CT26-CCL3 or CT26-CXCL9 tumor cells, and tumor size was measured every 3 days. Four mice per group. Data represent mean ± SEM (n=4). *p<0.05, **p<0.01.

Figure 4 shows the identification of CXCL9 and OX40L overexpression in mesenchymal stem cells. A, WB detection of CXCL9 overexpression in MSCs. B, ELISA detects the overexpression of CXCL9 in MSCs. Data represent mean ± SEM (n=3). ***p<0.001. C, WB detected the overexpression of OX40L in MSCs. D, The overexpression of OX40L in MSCs was detected by flow cytometry. E, Co-culture of MSC-OX40L with spleen cells stimulates the proliferation of splenic T cells.

Figure 5 shows that mesenchymal stem cells overexpressing CXCL9 and OX40L inhibit the growth of subcutaneous xenografts. A, ELISA to detect the secretion of CXCL9. B, The expression of OX40L was detected by flow cytometry. C, Figure shows the size of CT26 subcutaneous xenografts at different time points. Arrows indicate the corresponding times of PBS or MSC injections into mice. Data represent mean ± SEM (n=5). D, Flow cytometry analysis of the proportion of immune cells in the tumor after MSC treatment. *p<0.05, **p<0.01, ***p<0.001, ns=not significant.

Figure 6 shows that mesenchymal stem cells overexpressing CXCL9 and OX40L inhibit AOM/DSS-induced colorectal cancer. A, Schematic diagram of AOM/DSS treatment and MSC treatment. B, Representative images of colorectal tumors. Scale bar: 5mm. C, Mean tumor number and size. Data represent mean ± SEM (n=3-4). *p<0.05, **p<0.01, ***p<0.001, ns=not significant. D, Immunofluorescence staining of CD8 and NK cells. Scale bar: 50 μm.

Figure 7 shows that PD-1 and CTLA-4 antibody combination therapy has no significant therapeutic efficacy on AOM/DSS-induced colorectal cancer. A, Schematic diagram of AOM/DSS treatment and antibody treatment protocol. B, Mean tumor number and size. Data represent mean ± SEM (n=4). ns=not significant.

Detailed ways

After extensive and in-depth research and extensive screening, the inventors unexpectedly discovered for the first time that mesenchymal stem cells overexpress chemokines CCL3, CCL19, CCL21, XCL1, CXCL9 and/or cytokines OX40L, 4-1BBL, GITRL, CD40L can specifically attract and activate immune cells that kill tumor tissue at the tumor site, and mesenchymal stem cells have a synergistic effect with chemokines and/or cytokines, resulting in more efficient immune efficacy with less side effects. In particular, when mesenchymal stem cells overexpress CXCL9 and OX40L, they have a synergistic effect and significantly enhance the killing ability of tumor tissues, especially colorectal cancer cells. On this basis, the inventors have completed the present invention.

In recent years, immunotherapies such as cytokines, CAR-T cells or immune checkpoint blockade have produced good effects in some cancer patients, but they have also encountered many obstacles, such as the low efficiency of T cells reaching the tumor site, and the existing tumor sites. The number of immune cells is low, and the side effects caused by systemic medication. Mesenchymal stem cells can be obtained from various tissues in vivo. The inventors' studies in mouse models confirmed that adipose-derived mesenchymal stem cells can specifically migrate to tumor sites and are not enriched in other organs, so they can be used as ideal drug carriers. The present invention utilizes adipose mesenchymal stem cells as carriers to overexpress chemokine CXCL9 and cytokine OX40L with immunoregulatory effects, and through active migration of mesenchymal stem cells to tumors, specifically attracts and activates the immune system that kills tumor tissues at tumor sites cells, and ultimately achieve more efficient immunotherapy efficacy with less side effects.

Glossary

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.

As used herein, when used in reference to a specifically recited value, the term "about" means that the value may vary by no more than 1% from the recited value. For example, as used herein, the expression "about 100" includes all values between 99 and 101 and (eg, 99.1, 99.2, 99.3, 99.4, etc.).

As used herein, the terms "containing" or "including (including)" can be open, semi-closed, and closed. In other words, the term also includes "consisting essentially of," or "consisting of."

As used herein, the term "administration" refers to the physical introduction of a product of the present invention into a subject using any of a variety of methods and delivery systems known to those of skill in the art, including intravenous, intramuscular, subcutaneous, peritoneal Intra, spinal or other parenteral routes of administration, for example by injection or infusion.

Mesenchymal Stem Cells (MSCs)

Mesenchymal stem cells (MSCs) have emerged in recent years as a potential cell carrier with active migration ability against many different tumor types when administered systemically. It can be extracted from many different adult tissues, can be easily expanded and cultured, and can avoid immune rejection. At the same time, the tumor-tropic migration characteristics of MSCs and their ability to survive long-term at targeted sites make them an important resource for cell therapy. Common types of MSCs are bone marrow-derived MSCs (BM-MSCs), umbilical cord blood-derived MSCs (UCB-MSCs), umbilical cord-derived MSCs (UC-MSCs), and adipose tissue-derived MSCs (AT-MSCs). However, the separation process of BM-MSCs and UCB-MSCs is complicated and inefficient. Therefore, adipose tissue or umbilical cord tissue MSCs can be a more ideal alternative because they contain more MSCs than bone marrow and umbilical cord blood, and the tissue is easier to obtain and collect. Furthermore, with regard to the source of autologous stem cells for personalized cell therapy, AT-MSCs have minimal risk to the donor and no ethical concerns.

Through the tumor homing ability of MSCs, the present invention utilizes MSC to target and deliver chemokines CCL3, CCL21, XCL1, CXCL9 and cytokines OX40L, 4-1BBL, GITRL, CD40L to attract and activate effector T cells in the tumor microenvironment, NK cells and antigen-presenting cells, resulting in a more precise and sustained immune response to kill tumor cells. In the current study, adipose-derived mesenchymal stem cells were used as vectors to overexpress chemokines and cytokines to treat colorectal cancer in a mouse model.

expression cassette

As used herein, an "expression cassette" or "expression cassette of the invention" includes a first expression cassette and/or a second expression cassette. The first expression cassette contains a nucleic acid sequence of a chemokine; the second expression cassette contains a nucleic acid sequence encoding a cytokine, wherein the chemokine includes: CCL3, CCL19, CCL21, XCL1, CXCL9, or a combination thereof , the cytokines include: OX40L, 4-1BBL, GITRL, CD40L, or a combination thereof.

In one embodiment, the exogenous nucleic acid molecule comprises a first expression cassette containing a nucleic acid sequence encoding CXCL9 and a second expression cassette containing a nucleic acid sequence encoding OX40L.

In another preferred embodiment, the first expression cassette and the second expression cassette are independent of each other, or combined into one. In another preferred embodiment, the first expression cassette and the second expression cassette further comprise a promoter and/or a terminator, respectively. In another preferred embodiment, the first expression cassette and the second expression cassette are located on a vector or integrated into the chromosome of the mesenchymal stem cell. In another preferred embodiment, the first expression cassette and the second expression cassette are located on the same or different vectors. In another preferred embodiment, the first expression cassette and the second expression cassette are located in the same vector. In another preferred embodiment, the vector is selected from the group consisting of DNA, RNA, plasmid, lentiviral vector, adenoviral vector, retroviral vector, transposon, other gene transfer systems, or a combination thereof.

carrier

The present invention also provides a vector containing the expression cassette of the present invention. Vectors derived from retroviruses such as lentiviruses are suitable tools to achieve long-term gene transfer because they allow long-term, stable integration of the transgene and its proliferation in daughter cells. Lentiviral vectors have advantages over vectors derived from oncogenic retroviruses such as murine leukemia virus because they can transduce non-proliferating cells such as hepatocytes. They also have the advantage of low immunogenicity.

Briefly summarized, generally by operably linking an expression cassette or nucleic acid sequence of the invention to a promoter, and incorporating it into an expression vector. The vector is suitable for replication and integration in eukaryotic cells. Typical cloning vectors contain transcriptional and translational terminators, initial sequences and promoters that can be used to regulate the expression of the desired nucleic acid sequence.

The expression constructs of the present invention can also be used in nucleic acid immunization and gene therapy using standard gene delivery protocols. Methods of gene delivery are known in the art. See, eg, US Patent Nos. 5,399,346, 5,580,859, 5,589,466, which are hereby incorporated by reference in their entirety. In another embodiment, the present invention provides gene therapy vectors.

The expression cassette or nucleic acid sequence can be cloned into many types of vectors. For example, the expression cassette or nucleic acid sequence can be cloned into vectors including, but not limited to, plasmids, phagemids, phage derivatives, animal viruses, and cosmids. Particular vectors of interest include expression vectors, replication vectors, probe generation vectors, and sequencing vectors.

Further, expression vectors can be provided to cells in the form of viral vectors. Viral vector technology is well known in the art and described, for example, in Sambrook et al. (2001, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, New York) and other virology and molecular biology manuals. Viruses that can be used as vectors include, but are not limited to, retroviruses, adenoviruses, adeno-associated viruses, herpesviruses, and lentiviruses. In general, suitable vectors contain an origin of replication functional in at least one organism, a promoter sequence, convenient restriction enzyme sites, and one or more selectable markers (eg, WO01/96584; WO01/29058; and U.S. Patent No. 6,326,193).

A number of virus-based systems have been developed for gene transfer into mammalian cells. For example, retroviruses provide a convenient platform for gene delivery systems. The selected gene can be inserted into a vector and packaged into retroviral particles using techniques known in the art. The recombinant virus can then be isolated and delivered to subject cells in vivo or ex vivo. Many retroviral systems are known in the art.

Additional promoter elements, such as enhancers, can regulate the frequency of transcription initiation. Typically, these are located in a region of 30-110 bp upstream of the initiation site, although it has recently been shown that many promoters also contain functional elements downstream of the initiation site. The spacing between promoter elements is often flexible so that promoter function is maintained when elements are inverted or moved relative to one another. In the thymidine kinase (tk) promoter, the spacing between promoter elements can be increased by 50 bp before activity begins to decline. Depending on the promoter, individual elements appear to act cooperatively or independently to initiate transcription.

An example of a suitable promoter is the early cytomegalovirus (CMV) promoter sequence. The promoter sequence is a strong constitutive promoter sequence capable of driving high-level expression of any polynucleotide sequence operably linked thereto. Another example of a suitable promoter is elongation growth factor-1α (EF-1α). However, other constitutive promoter sequences can also be used, including but not limited to the simian virus 40 (SV40) early promoter, the mouse breast cancer virus (MMTV), the human immunodeficiency virus (HIV) long terminal repeat (LTR) promoter, MoMuLV promoter, avian leukemia virus promoter, Epstein-Barr virus immediate early promoter, Russell sarcoma virus promoter, and human gene promoters such as, but not limited to, the actin promoter , myosin promoter, heme promoter and creatine kinase promoter. Further, the present invention should not be limited to the use of constitutive promoters. Inducible promoters are also contemplated as part of the present invention. The use of an inducible promoter provides a molecular switch that can turn on expression of a polynucleotide sequence operably linked to an inducible promoter when such expression is desired, or turn off expression when expression is not desired. Examples of inducible promoters include, but are not limited to, metallothionein promoters, glucocorticoid promoters, progesterone promoters, and tetracycline promoters.

Expression vectors introduced into cells may also contain either or both selectable marker genes or reporter genes to facilitate identification and selection of expressing cells from a population of cells sought to be transfected or infected by the viral vector. In other aspects, the selectable marker can be carried on a single piece of DNA and used in co-transfection procedures. Both the selectable marker and the reporter gene can be flanked by appropriate regulatory sequences to enable expression in the host cell. Useful selectable markers include, for example, antibiotic resistance genes such as neo and the like.

Reporter genes are used to identify potentially transfected cells and to evaluate the functionality of regulatory sequences. Typically, a reporter gene is a gene that is not present in or expressed by the recipient organism or tissue and that encodes a polypeptide whose expression is clearly indicated by some readily detectable property such as enzymatic activity. After the DNA has been introduced into the recipient cells, the expression of the reporter gene is measured at an appropriate time. Suitable reporter genes can include genes encoding luciferase, beta-galactosidase, chloramphenicol acetyltransferase, secreted alkaline phosphatase, or green fluorescent protein genes (eg, Ui-Tei et al., 2000 FEBS Letters 479: 79-82). Suitable expression systems are well known and can be prepared using known techniques or obtained commercially. Typically, constructs with a minimum of 5 flanking regions showing the highest levels of reporter gene expression are identified as promoters. Such promoter regions can be linked to reporter genes and used to assess the ability of an agent to modulate promoter-driven transcription.

Methods for introducing and expressing genes into cells are known in the art. In the context of an expression vector, the vector can be readily introduced into a host cell, eg, mammalian (eg, human T cells), bacterial, yeast, or insect cells, by any method known in the art. For example, an expression vector can be transferred into a host cell by physical, chemical or biological means.

Physical methods of introducing polynucleotides into host cells include calcium phosphate precipitation, lipofection, particle bombardment, microinjection, electroporation, and the like. Methods of producing cells comprising vectors and/or exogenous nucleic acids are well known in the art. See, eg, Sambrook et al. (2001, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, New York).

Biological methods for introducing polynucleotides into host cells include the use of DNA and RNA vectors. Viral vectors, especially retroviral vectors, have become the most widely used method of inserting genes into mammalian, eg, human cells. Other viral vectors can be derived from lentiviruses, poxviruses, herpes simplex virus I, adenoviruses and adeno-associated viruses, among others. See, eg, US Patent Nos. 5,350,674 and 5,585,362.

Chemical means of introducing polynucleotides into host cells include colloidal dispersion systems, such as macromolecular complexes, nanocapsules, microspheres, beads; and lipid-based systems, including oil-in-water emulsions, micelles, mixed micelles, and lipids plastid. Exemplary colloidal systems for use as in vitro and in vivo delivery vehicles are liposomes (eg, artificial membrane vesicles).

Where non-viral delivery systems are used, exemplary delivery vehicles are liposomes. The use of lipid formulations is contemplated to introduce nucleic acids into host cells (in vitro, ex vivo, or in vivo). In another aspect, the nucleic acid can be associated with a lipid. Nucleic acids associated with lipids can be encapsulated into the aqueous interior of liposomes, interspersed within the lipid bilayer of liposomes, attached via linker molecules associated with both liposomes and oligonucleotides to liposomes, entrapped in liposomes, complexed with liposomes, dispersed in lipid-containing solutions, mixed with lipids, associated with lipids, contained in lipids as a suspension, contained in micelles or Complex with micelles, or otherwise associated with lipids. The lipid, lipid/DNA or lipid/expression vector associated with the composition is not limited to any particular structure in solution. For example, they may exist in bilayer structures, as micelles or have a "collapsed" structure. They can also simply be dispersed in solution, possibly forming aggregates that are not uniform in size or shape. Lipids are fatty substances, which can be naturally occurring or synthetic lipids. For example, lipids include lipid droplets, which occur naturally in the cytoplasm as well as in such compounds comprising long chain aliphatic hydrocarbons and their derivatives such as fatty acids, alcohols, amines, amino alcohols and aldehydes.

Preparation

The present invention provides a method for preparing mesenchymal stem cells, comprising introducing a first expression cassette and/or a second expression cassette into the mesenchymal stem cells to be engineered, wherein the first expression cassette is used to express chemotaxis cytokines, and the second expression cassette is used to express cytokines, thereby obtaining the mesenchymal stem cells.

It generally includes the following steps: (1) transforming or transducing a suitable host cell with a polynucleotide encoding the immunostimulatory factor of the present invention, or with a recombinant expression vector containing the polynucleotide; (2) culturing in a suitable medium of host cells.

preparation

The present invention provides a mesenchymal stem cell according to the first aspect of the present invention, and a pharmaceutically acceptable carrier, diluent or excipient. In one embodiment, the formulation is a liquid formulation. Preferably, the formulation is an injection. Preferably, the concentration of the mesenchymal stem cells in the preparation is 1×10 ³ -1×10 ⁸ cells/ml, more preferably 1×10 ⁴ -1×10 ⁷ cells/ml.

In one embodiment, the formulation may include buffers such as neutral buffered saline, sulfate buffered saline, etc.; carbohydrates such as glucose, mannose, sucrose or dextran, mannitol; proteins; polypeptides or amino acids such as glycine ; antioxidants; chelating agents such as EDTA or glutathione; adjuvants (eg, aluminum hydroxide); and preservatives. The formulations of the present invention are preferably formulated for intravenous administration.

therapeutic application

The present invention includes the therapeutic use of mesenchymal stem cells transduced with the vector containing the expression cassette of the present invention. The mesenchymal stem cells of the present invention can actively migrate to the tumor site, and are not enriched in organs such as liver, spleen, kidney, etc., and have the specificity and safety as a drug carrier for tumor treatment. Sexual side effects provide an effective means. The adipose-derived mesenchymal stem cell therapy system overexpressing chemokine CXCL9 and cytokine OX40L has the characteristics of specific targeting to tumor sites, and can attract and activate T cells and NK cells to achieve ideal anti-tumor efficacy.

In one embodiment, the present invention provides a type of cell therapy comprising administering to a mammal the mesenchymal stem cells of the present invention. Unlike antibody therapy, the mesenchymal stem cells of the present invention are capable of replicating in vivo, resulting in long-term persistence that can lead to sustained tumor control.

Cancers that can be treated include tumors that are not vascularized or substantially not vascularized, as well as tumors that are vascularized. Cancers may include non-solid tumors (such as hematological tumors, eg, leukemias and lymphomas) or may include solid tumors. Cancer types to be treated with the mesenchymal stem cells of the invention include, but are not limited to, carcinomas, blastomas and sarcomas, and certain leukemia or lymphoid malignancies, benign and malignant tumors, and malignant tumors such as sarcomas, carcinomas and melanomas . Also includes adult tumors/cancers and pediatric tumors/cancers.

Hematological cancers are cancers of the blood or bone marrow. Examples of hematological (or hematogenous) cancers include leukemias, including acute leukemias (such as acute lymphoblastic leukemia, acute myeloid leukemia, acute myeloid leukemia, and myeloblastoid, promyelocytic, myelomonocytic type) , monocytic and erythroleukemia), chronic leukemia (such as chronic myeloid (myeloid) leukemia, chronic myelogenous leukemia, and chronic lymphocytic leukemia), polycythemia vera, lymphoma, Hodgkin's disease, non- Hodgkin's lymphoma (painless and high-grade forms), multiple myeloma, Waldenstrom's macroglobulinemia, heavy chain disease, myelodysplastic syndrome, hairy cell leukemia, and myelodysplasia.

Solid tumors are abnormal masses of tissue that typically do not contain cysts or areas of fluid. Solid tumors can be benign or malignant. Different types of solid tumors are named after the cell type that forms them (such as sarcomas, carcinomas, and lymphomas). Examples of solid tumors such as sarcomas and carcinomas include fibrosarcoma, myxosarcoma, liposarcoma, mesothelioma, lymphoid malignancies, pancreatic cancer, and ovarian cancer.

The mesenchymal stem cells of the present invention can also be used as a type of vaccine for ex vivo immunization and/or in vivo therapy of mammals. Preferably, the mammal is a human.

For ex vivo immunization, at least one of the following occurs in vitro prior to administering the cells into a mammal: i) expanding the cells, ii) introducing the expression cassettes of the invention into the cells, and/or iii) cryopreserving the cells.

Ex vivo procedures are well known in the art and are discussed more fully below. Briefly, cells are isolated from mammals (preferably human) and genetically modified (ie, transduced or transfected in vitro) with vectors containing the expression cassettes of the invention. The mesenchymal stem cells of the present invention can be administered to a mammalian recipient to provide therapeutic benefit. The mammalian recipient can be a human, and the mesenchymal stem cells of the invention can be autologous to the recipient. Alternatively, the cells may be allogeneic, syngeneic or xenogeneic with respect to the recipient.

In addition to using cell-based vaccines for ex vivo immunization, the present invention also provides compositions and methods for in vivo immunization to elicit an immune response against an antigen in a patient.

Generally, cells activated and expanded as described herein can be used to treat and prevent diseases that arise in individuals who are immunocompromised. Accordingly, the present invention provides a method of treating cancer comprising administering to a subject in need thereof a therapeutically effective amount of mesenchymal stem cells of the present invention.

The mesenchymal stem cells of the present invention can be administered alone or as a pharmaceutical composition in combination with diluents and/or with other components such as certain cytokines or cell populations. Briefly, a pharmaceutical composition or formulation of the present invention may include mesenchymal stem cells as described herein, in combination with one or more pharmaceutically or physiologically acceptable carriers, diluents or excipients.

The pharmaceutical compositions of the present invention can be administered in a manner appropriate to the disease to be treated (or prevented). The amount and frequency of administration will be determined by factors such as the patient's condition, and the type and severity of the patient's disease - although appropriate doses may be determined by clinical trials.

When referring to an "immunologically effective amount", "anti-tumor effective amount", "tumor-suppressive effective amount" or "therapeutic amount", the precise amount of the composition of the invention to be administered can be determined by a physician, taking into account the patient (subject ) individual differences in age, weight, tumor size, degree of infection or metastasis, and condition. It may generally be noted that the pharmaceutical compositions comprising the mesenchymal stem cells described herein may be administered at a dose of 10 ⁴ to 10 ⁹ cells/kg body weight, preferably 10 ⁵ to 10 ⁶ cells/kg body weight (including those within those ranges). all integer values) are administered. The mesenchymal stem cell composition can also be administered multiple times at these doses. Cells can be administered using infusion techniques well known in immunotherapy (see, eg, Rosenberg et al., New Eng. J. of Med. 319:1676, 1988). Optimal dosages and treatment regimens for a particular patient can be readily determined by those skilled in the medical arts by monitoring the patient for signs of disease and adjusting treatment accordingly.

Administration of the composition to a subject can be carried out in any convenient manner, including by nebulization, injection, swallowing, infusion, implantation, or transplantation. The compositions described herein can be administered to a patient subcutaneously, intradermally, intratumorally, intranodal, intraspinal, intramuscularly, by intravenous (i.v.) injection, or intraperitoneally. In one embodiment, the T cell composition of the present invention is administered to a patient by intradermal or subcutaneous injection. In another embodiment, the T cell composition of the present invention is preferably administered by i.v. injection. Compositions of mesenchymal stem cells can be injected directly into tumors, lymph nodes, or sites of infection.

In certain embodiments of the invention, cells activated and expanded using the methods described herein, or other methods known in the art to expand mesenchymal stem cells to therapeutic levels, are combined with any number of relevant therapeutic modalities (e.g. , before, at the same time, or after) administration to a patient in a form of treatment including, but not limited to, treatment with agents such as antiviral therapy, cidofovir and interleukin-2, cytarabine (also Known as ARA-C) or natalizumab therapy for MS patients or elfazizumab therapy for psoriasis patients or other treatments for PML patients. In a further embodiment, the mesenchymal stem cells of the present invention may be used in combination with chemotherapy, radiation, immunosuppressive agents such as cyclosporine, azathioprine, methotrexate, mycophenolate mofetil and FK506 , antibodies or other immunotherapeutics. In a further embodiment, the cellular composition of the invention is administered in combination with (eg, before, concurrently or after) bone marrow transplantation, using chemotherapeutic agents such as fludarabine, external beam radiation therapy (XRT), cyclophosphamide patient. For example, in one embodiment, the subject may undergo standard treatment with high dose chemotherapy followed by peripheral blood stem cell transplantation. In some embodiments, after transplantation, the subject receives an infusion of expanded mesenchymal stem cells of the invention. In an additional embodiment, the expanded cells are administered before or after surgery.

The dosage of the above treatments administered to a patient will vary with the precise nature of the condition being treated and the recipient of the treatment. Dosage ratios for human administration can be carried out in accordance with art-accepted practice. Typically, 1 x 10 ³ to 1 x 10 ¹⁰ mesenchymal stem cells of the present invention may be administered to a patient, eg, by intravenous infusion, per treatment or per course of treatment.

The technical scheme of the present invention has the following beneficial effects:

1. The mesenchymal stem cells of the present invention can be obtained from various tissues in vivo, and are easy to be cultured, expanded and transformed by genetic engineering methods in vitro, and have low immunogenicity.

2. Compared with most immunotherapies, the method of the present invention does not depend on the presence of tumor-infiltrating lymphocytes, and is also suitable for the treatment of tumors with very low or resistant lymphocyte infiltration in clinical practice.

3. When the mesenchymal stem cells of the present invention overexpress one or more of CCL3, CCL19, CCL21, XCL1, CXCL9, OX40L, 4-1BBL, GITRL, and CD40L, they can specifically attract and activate and kill tumor tissue at the tumor site The immune cells have more efficient and less side effects of immune efficacy.

4. When the mesenchymal stem cells of the present invention overexpress CXCL9 and OX40L, there is a synergistic effect, and the killing ability of tumor tissue is significantly enhanced, especially colorectal cancer cells. This method also has a killing effect on MHC-I-negative tumor cells that are resistant to traditional immunotherapy (such as CAR-T or PD-1/PD-L1 antibodies).

5. When the present invention is used in combination with other immunotherapies used in the clinic, such as CAR-T or PD-1/PD-L1 antibodies, the efficacy of these immunotherapies can also be enhanced.

The present invention will be further described below in conjunction with specific implementation. It should be understood that these examples are only used to illustrate the present invention and not to limit the scope of the present invention. The experimental method of unreceipted specific conditions in the following examples, usually according to normal conditions, such as people such as Sambrook, molecular cloning: conditions described in laboratory manual (New York:Cold Spring Harbor LaboratoryPress, 1989), or according to manufacturer the proposed conditions. Percentages and parts are by weight unless otherwise indicated.

Materials and methods

cell line

CT26 cells were colon adenocarcinoma cells derived from BALB/c mice and were purchased from Shanghai Institutes for Biological Sciences. CT26 cells were cultured in RPMI 1640 containing 10% fetal bovine serum and 1% penicillin/streptomycin.

Antibody

Antibodies used for flow cytometry were obtained from BD Biosciences, BioLegend or eBioscience. Antibodies used for western blot analysis included anti-CCL3 (R&D Systems), anti-CXCL9 (Abcam), anti-Myc-tag (Cell Signaling Technology), anti-OX40L (Abcam) and anti-GAPDH (Abcam). Antibodies for immunofluorescence staining included anti-GFP (Abcam), anti-CD8a (BioLegend) and anti-NKp46 (CD335) (BioLegend).

Immune checkpoint blocking antibodies anti-PD-1 (clone RMP1-4) and anti-CTLA-4 (clone9D9) were purchased from Bio X Cell. The two antibodies (anti-PD-1: 200 μg/mouse; anti-CTLA-4: 100 μg/mouse) were administered to mice by intraperitoneal injection.

Isolation, Culture and Characterization of Mesenchymal Stem Cells from Mouse Adipose Tissue

AT-MSCs were isolated by digesting mouse subcutaneous adipose tissue with type I collagenase. Cells were cultured in α-MEM medium containing 10% fetal bovine serum and 1% penicillin/streptomycin. The expression of cell surface marker proteins was identified by flow cytometry after the cells were adherently cultured for three passages.

Lentivirus Generation and Transduction

The cDNA was cloned into a lentiviral vector. Packaging and titer determination of lentiviruses were performed by Heyuan Biotechnology (Shanghai) Co., Ltd. Mesenchymal stem cells were infected with lentivirus at a multiplicity of infection (MOI) of 60 in the presence of 6 μg/ml polybrene (Sigma-Aldrich).

Tumor cell proliferation assay

The proliferation of tumor cells was measured using the CCK-8 kit (Dojindo Molecular Technologies) according to the instructions. Absorbance was measured using a microplate reader (Tecan).

Western Blotting

Cells were harvested and treated with cell lysis buffer (RIPA buffer + 1% protease inhibitors) (ThermoFisher Scientific) to prepare cell lysates. Protein concentrations in cell lysates were determined using the BCA kit (ThermoFisher Scientific). 15 to 30 micrograms of protein were loaded onto 5% to 15% SDS-PAGE protein gels (ThermoFisher Scientific) and then transferred to PVDF membranes (Millipore). Membranes were blocked with 5% nonfat milk prepared in TBST buffer and incubated overnight at 4°C with antibodies to Myc-tag, OX40L, CXCL9 and GAPDH. Membranes were washed with TBS-T buffer and incubated with horseradish peroxidase-conjugated secondary antibody for 1 h at room temperature. Membranes were developed and exposed to the enhanced chemiluminescence kit (Millipore).

Enzyme-linked immunosorbent assay (ELISA)

The supernatants of lentivirally transduced AT-MSCs were collected and stored in a −80 °C freezer until measurement. CXCL9 secretion was tested using an ELISA kit from Abcam according to the instructions.

T cell proliferation assay

T lymphocytes were isolated from mouse spleen using Pan T Cell Isolation Kit II (Miltenyi Biotec). Immediately after isolation, T cells were activated and expanded using a T cell activation/expansion kit (Miltenyi Biotec) containing CD3 and CD28 antibodies and an additional 20 ng/ml recombinant mouse IL-2 (R&D Systems). After 48 hours, cells were harvested and washed thoroughly.

To examine the effect of cytokine-overexpressing mAT-MSCs on T cell proliferation, lentivirus-transduced mAT-MSCs (2.5×10 ⁴ ) were seeded on 24-well plates and incubated at 37°C for 4 hours, and incubated with culture medium Wash 5 times. ¹ x 105 activated T cells labeled with CFSE (ThermoFisher Scientific) were then co-cultured with ^mAT -MSCs (2.5 x 104) in complete medium of RPMI1640. After 96 hours, T cell proliferation was detected by analyzing the fluorescence intensity of CFSE by flow cytometry.

Mouse subcutaneous tumor model

CT26 (0.5 or 1×10 ⁶ /mouse) cells were injected subcutaneously in the right lower back of 8- to 10-week-old BALB/c mice, respectively. When tumors reached 0.5 to 0.7 cm in maximum diameter, mice were randomly assigned to experimental groups. Systemic administration was performed by tail vein injection of 250 μl PBS or 250 μl PBS suspension containing 5×10 ⁵ AT-MSCs per animal. Tumor size was measured with a vernier caliper every three days, and tumor volume was calculated using the formula: V = L x W ² /2, where L and W are the long and short diameters of the tumor, respectively. The mice were monitored for tumor size and survival. Mice were sacrificed when the tumor volume reached 2 ^cm3 or when the tumor became ulcerated or the mice were dying.

Streaming Analysis

To identify AT-MSCs, adherent cells at passages 3 to 5 were isolated by digestion with 20 μM EDTA, then washed twice with PBS and stained with antibodies.

For analysis of tumor-infiltrating immune cells, subcutaneously implanted tumors were dissected and transferred into RPMI medium, minced with scissors, and placed in a medium containing 0.25 mg/ml Liberase TL (Roche) and 50 μg/ml DNase I (Sigma- Aldrich) serum-free RPMI medium, digested at 37°C using gentleMAC Octo Dissociator (Milteniy Biotec) and dispersed through a 40 μm cell strainer (BD Biosciences). Single cells were further washed and stained with antibodies. Dead cells were excluded by staining with Zombie Fixable Viability Kit (BioLegend). For intracellular staining for cytokines, each mouse was injected intraperitoneally with 0.25 mg Brefeldin A (BFA) (Selleck) 4-6 hours before harvesting the samples. After surface staining in the presence of 5 μg/ml BFA, intracellular staining was performed with an intracellular fixation and permeabilization buffer set (eBioscience). Surface staining was followed by nuclear staining with Foxp3 transcription factor staining buffer (eBioscience).

Flow data were acquired on a BD LSRFortessa Cell Analyzer (BD Biosciences) and analyzed using FlowJo software. All antibodies used for flow cytometry were purchased from BD Biosciences, BioLegend or eBioscience.

AOM/DSS-induced mouse colorectal cancer model

BALB/c mice were injected intraperitoneally with AOM (12.5 mg/kg body weight; Sigma-Aldrich) (14). After 1 week, mice were given drinking water containing 3% DSS (MP Biomedicals) for 7 days, followed by normal water for 2 weeks. DSS induction continued for two cycles and mice were sacrificed after five injections of MSCs via tail vein starting from the last week of the DSS induction cycle. Body weight was recorded during DSS treatment. Colons were removed from mice, rinsed with ice-cold PBS, opened longitudinally, fixed in 4% paraformaldehyde solution (Sigma-Aldrich) overnight at room temperature, and paraffin embedded. Before fixing, use digital calipers to take dimension measurements.

Immunofluorescence

Tissue sections were blocked with 10% normal goat serum and then incubated with primary antibodies overnight at 4°C and secondary antibodies for 1 hour at room temperature. Slides were mounted in fade-resistant mounting medium with DAPI (ThermoFisher Scientific) and observed under a Nikon Eclipse Ti fluorescence microscope. Antibodies used for immunofluorescence were GFP antibody (Abeam), CD8a antibody (BioLegend) and NKp46 antibody (CD335) (BioLegend).

statistics

All results are expressed as mean ± SEM. Differences were assessed by Student's t-test, or when comparing the means of more than two groups, by two-way ANOVA followed by Bonferroni's multiple comparisons test. Data analysis was performed with Prism software (GraphPad). Statistical significance was set at the level of P<0.05.

Study Approval

All animal procedures were approved by the Animal Care and Use Committee of Shanghai Jiao Tong University.

Example 1 Characteristics of adipose-derived mesenchymal stem cells migrating to tumors

Mesenchymal stem cells were extracted from mouse subcutaneous adipose, and detected by flow cytometry, these cells expressed specific mesenchymal stem cell marker molecules and did not express marker molecules of other cell types (Fig. 1A), confirming that the adipose tissue used for the experiment was Purity of mesenchymal stem cells. Adipose-derived mesenchymal stem cells were transfected with lentivirus to express GFP, and 5×10 ⁵ cells were injected into tumor-bearing mice (CT26 intestinal cancer subcutaneous tumor) through the tail vein. After 7 days, the tumor and other organs were organized. Immunofluorescence staining of the sections showed that GFP-positive mesenchymal stem cells only resided in tumors, but were not found in other organs such as liver, spleen, and kidney (Fig. 1B). GFP-positive mesenchymal stem cells in tumors were detected by flow cytometry, and a certain number of cells could still be detected 14 days after cell infusion (Fig. 1C). These results demonstrate that adipose-derived mesenchymal stem cells can specifically migrate to tumor sites and reside for a long time, supporting their potential as carriers of therapeutic molecules.

Example 2 Antitumor properties of CXCL9 and OX40L

In order to search for immune-activating therapeutic molecules with high efficacy, chemokines and cytokines with potential anti-tumor functions were selected, and the genes were cloned into lentiviral vectors to package lentiviruses carrying these genes. The CT26 intestinal cancer cell lines transduced with these genes or blank control lentiviruses were subjected to subcutaneous transplantation tumor experiments to detect the antitumor efficacy of these molecules. After overexpression of the chemokines CCL3 and CXCL9 with potential antitumor efficacy in CT26 (Fig. 2A), neither cell proliferation was affected in vitro (Fig. 2B), while the growth of subcutaneous xenografts in vivo was significantly inhibited (Fig. 2C), indicating that these chemokines may inhibit tumor growth through the action of the immune system in vivo. Among them, CXCL9 has the most significant anti-tumor effect. Detection of immune cell composition in tumors by flow cytometry revealed that CXCL9 indeed enhanced the infiltration of anti-tumor immune cells such as CD8, CD4 and NK (Fig. 2D).

In CT26 cells overexpressing two immune-activating cytokines, IL36β and OX40L (Fig. 3A&B), it was also found that overexpression of these two cytokines had no effect on tumor cell proliferation in vitro (Fig. 3C), and subcutaneously transplanted tumor growth It has an obvious inhibitory effect (Figure 3D), which also indicates that the anti-tumor effect may be achieved through the immune system in vivo. Among them, OX40L showed strong anti-tumor efficacy.

Example 3 Anti-tumor efficacy of mesenchymal stem cells overexpressing chemokine CXCL9 and cytokine OX40L

A adipose-derived mesenchymal stem cell system overexpressing CXCL9 and OX40L was established by lentiviral infection. The successful expression and secretion of CXCL9 were identified by western blotting and ELISA techniques (Figure 4A&B), and the successful expression of OX40L on the cell membrane was confirmed by western blotting and flow cytometry (Figure 4C&D). Mesenchymal stem cells overexpressing OX40L were also able to stimulate the proliferation of T cells after co-culture with T cells (Fig. 4E), demonstrating its biological activity. Afterwards, MSCs overexpressing CXCL9 and OX40L were established (Fig. 5A & B). In the CT26 subcutaneous xenograft model, mice were injected with 5 × 10 ⁵ mesenchymal stem cells or PBS each time through the tail vein, after four days between each time. After a total of three treatments, mesenchymal stem cells harboring both CXCL9 and OX40L exhibited the strongest antitumor efficacy (Fig. 5C). Flow cytometry analysis found that the proportion of lymphocytes, especially anti-tumor CD8 T cells and NK cells in the tumor was significantly increased (Fig. 5D), indicating that the therapy effectively activated the anti-tumor immune response.

In order to further explore the efficacy of the mesenchymal stem cell immunotherapy system, AOM/DSS was used to induce an orthotopic colorectal cancer model caused by inflammation. Starting from the last week of the third DSS treatment cycle, mice were treated for a total of 5 times for 4 weeks. Treatment (Fig. 6A), with PBS or 5 x 10 ⁵ MSCs per injection via tail vein, CXCL9- and OX40L-loaded MSCs resulted in an extremely significant reduction in intestinal tumors in mice (Fig. 6B&C) . Immunofluorescence staining demonstrated a marked increase in infiltration of anti-tumor CD8 T cells and NK cells (Fig. 6D), consistent with the results observed in the xenograft model.

All the above results indicated that adipose-derived mesenchymal stem cells overexpressing CXCL9 and OX40L exhibited extremely significant therapeutic effects in mouse models of subcutaneous xenografts and inflammation-induced orthotopic colorectal cancer. Mesenchymal stem cells that carry both CXCL9 and OX40L at the same time express CXCL9 and OX40L. The two have a synergistic effect, and the anti-tumor effect is significantly better than the anti-tumor effect of mesenchymal stem cells that express CXCL9 or OX40L alone.

discuss

Immunotherapy has revolutionized the treatment of cancer. Although some cytokines and immune checkpoint blockers have shown significant efficacy in the clinical treatment of tumors, systemic use of these drugs will non-specifically activate the immune system and affect most organs. In order to solve the side effects caused by systemic administration, mesenchymal stem cells were selected as drug carriers. The research results show that adipose-derived mesenchymal stem cells can actively migrate to the tumor site and are not enriched in the liver, spleen, kidney and other organs, which fully supports the specificity and safety of mesenchymal stem cells as a drug carrier for tumor therapy. Local activation of immune responses in tumors provides an effective means to avoid systemic side effects.

T cell and NK cell infiltration in tumors is a key determinant of the efficacy of immunotherapy in solid tumors. Tumors can restrict the infiltration of lymphocytes by different mechanisms. Tumors with more T cell infiltration often also highly express chemokines that can attract T cells, including CCL3, CCL4, and CXCL10. The present invention unexpectedly found that the use of mesenchymal stem cells as a carrier to express CXCL9 and transport it to the tumor site to attract anti-tumor lymphocytes shows stronger T cell and NK cell attraction ability, and solves the problem that lymphocytes are difficult to enter solid tumors. problem. In addition, loading OX40L in the mesenchymal stem cell system can also activate T cells and NK cells more efficiently. Activating antibodies to the OX40 receptor have entered the clinical stage (ClinicalTrials.gov), but potential problems are also the side effects of systemic medication. The ligand of OX40, OX40L, is a membrane protein. When expressed in mesenchymal stem cells, it can be directed and transported to the tumor site without being secreted like secreted cytokines and transferred to other sites, reducing the diffusion caused by secretion. It can activate existing or newly migrated lymphocytes at the tumor site. The present invention also unexpectedly found that adipose-derived mesenchymal stem cells overexpressing CXCL9 and OX40L exhibited extremely significant therapeutic effects in mouse subcutaneous transplanted tumors and inflammation-induced in situ colorectal cancer models.

Overall, the adipose-derived mesenchymal stem cell treatment system overexpressing chemokine CXCL9 and cytokine OX40L established in the present invention has the characteristics of specifically targeting tumor sites, and can attract and activate T cells and NK cells to achieve an ideal anti-tumor effect. tumor efficacy. In contrast to most immunotherapies, this therapy does not depend on the presence of tumor-infiltrating lymphocytes and is clinically suitable for the treatment of tumors with very low or resistant lymphocyte infiltration. Adipose or umbilical cord mesenchymal stem cells are easy to extract and culture, and can be easily applied to individualized treatment. Its low immunogenicity also makes allogeneic use feasible. Therefore, the established mesenchymal stem cell-based immunotherapy has extremely high clinical translation value.

All documents mentioned herein are incorporated by reference in this application as if each document were individually incorporated by reference. In addition, it should be understood that after reading the above teaching content of the present invention, those skilled in the art can make various changes or modifications to the present invention, and these equivalent forms also fall within the scope defined by the appended claims of the present application.

Claims (10)

1. A mesenchymal stem cell expressing an immunostimulatory factor selected from the group consisting of: CCL3, CCL19, CCL21, XCL1, CXCL9, OX40L, 4-1BBL, GITRL, CD40L, or a combination thereof.

2. The mesenchymal stem cell of claim 1, wherein the immunostimulatory factor comprises at least one chemokine, wherein the chemokine comprises: CCL3, CCL19, CCL21, XCL1, CXCL9, or a combination thereof; and/or

The immunostimulatory factor includes at least one cytokine, the cytokine including: OX40L, 4-1BBL, GITRL, CD40L, or a combination thereof.

3. The mesenchymal stem cell of claim 1, wherein the immunostimulatory factor is a combination of one or both of CCL3, CCL19, CCL21, XCL1 and CD 40L; or

The immunostimulant is one or two of OX40L, 4-1BBL and GITRL combined with CXCL 9.

4. The mesenchymal stem cell of claim 1, wherein the mesenchymal stem cell comprises: adipose mesenchymal stem cells, umbilical cord mesenchymal stem cells, or a combination thereof.

5. A method of preparing the mesenchymal stem cell of claim 1, comprising the steps of:

(1) providing a mesenchymal stem cell to be modified; and

(2) introducing an exogenous nucleic acid comprising a nucleic acid sequence encoding an immunostimulatory factor into the mesenchymal stem cell to be engineered, thereby obtaining the mesenchymal stem cell of claim 1;

Wherein the immunostimulatory factor is selected from the group consisting of: CCL3, CCL19, CCL21, XCL1, CXCL9, OX40L, 4-1BBL, GITRL, CD40L, or a combination thereof.

6. A formulation comprising the mesenchymal stem cell of claim 1, and a pharmaceutically acceptable carrier, diluent or excipient.

7. Use of mesenchymal stem cells according to claim 1, for the preparation of a medicament or formulation for the prevention and/or treatment of cancer or tumour.

8. Use according to claim 7, wherein in another preferred embodiment the tumour is a solid tumour, preferably colorectal cancer.

9. A pharmaceutical composition comprising

(1) The mesenchymal stem cell of claim 1; and

(2) an anti-tumor immunotherapeutic agent.

10. The pharmaceutical combination of claim 9, wherein the anti-tumor immunotherapeutic agent is an immune checkpoint antibody.

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